Regulatory Affairs Specialist - Hampshire

Up to £55,000 per annum plus benefits - Regulatory Affairs - Devices - Regulatory Affairs
Ref: 18 Date Posted: Thursday 12 Sep 2019
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Regulatory Affairs Specialist

Hampshire

Medical Device company

Up to £55k plus highly competitive benefits package

 

Our client offers an excellent opportunity to join a growing UK based medical device manufacturer with huge investment.

 

Due to continued and consistent growth and the investment to sell their product globally they have created a new position for a Regulatory Affairs Specialist to support the RA Manager and RA/QA Director.

 

This position will focus on global product registrations as well as supporting wider regulatory objectives within a team.

 

Our client offers a stable platform for employee learning & development as well as progression opportunities.

 

Position:

Global Product Registration / Regulatory Affairs Specialist

 

Location:

North Hampshire – ideal for someone residing in the Hampshire, Berkshire, Wiltshire, Surrey, M3 / M4, Oxfordshire area. *Relocation assistance available.

 

Salary:

Up to £55,000 per annum plus a highly attractive benefits package including bonus, a superb pension contribution and healthcare

 

Job role:

this role will focus on the registration of our client’s active medical device products globally. Further responsibilities include;

  • Technical files compilation
  • Clinical evaluation file compilation
  • Support product development teams throughout design control process
  • Preparation and submission of regulatory dossiers to agencies in EU, USA and Canada
  • Support regulatory team on other regulatory projects as required
  • Project manage own assigned projects

 

Ideal applicant skills / experience:

Our client is looking for a proven, senior level regulatory specialist or a regulatory officer looking to take a step up. Essential to this role is experience with medical device product registrations in multiple countries (outside of UK / EU). Further experience / skills required includes:

  • Degree level education or equivalent working experience within regulatory affairs
  • Excellent communication and presentation skills
  • Ability to work within a fast-paced environment with changing priorities

 

Job reference:

J-00013

 

Indo Professionals is a specialist medical device staffing business focused on placing high calibre professionals into regulatory affairs, quality assurance and clinical research positions UK wide. If you are looking for a new career challenge or would like a career consultation with an industry expert, please contact the team today.